Potent inhibitors of platelet aggregation based upon the Arg-Gly-Asp-Phe sequence of fibrinogen. A proposal on the nature of the binding interaction between the Asp-carboxylate of RGDX mimetics and the platelet GP IIb-IIIa receptor

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Veröffentlicht in:Journal of medicinal chemistry 1992-12, Vol.35 (26), p.4914-4917
Hauptverfasser: Zablocki, Jeffery A, Miyano, Masateru, Rao, Shashidhar N, Panzer-Knodle, Susan, Nicholson, Nancy, Feigen, Larry
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container_title Journal of medicinal chemistry
container_volume 35
creator Zablocki, Jeffery A
Miyano, Masateru
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Nicholson, Nancy
Feigen, Larry
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doi_str_mv 10.1021/jm00104a019
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ispartof Journal of medicinal chemistry, 1992-12, Vol.35 (26), p.4914-4917
issn 0022-2623
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source ACS Publications; MEDLINE
subjects Amino Acid Sequence
Fibrinogen - metabolism
Fibrinogen - pharmacology
Molecular Sequence Data
Oligopeptides - chemical synthesis
Oligopeptides - pharmacology
Platelet Aggregation - drug effects
Platelet Aggregation Inhibitors - chemical synthesis
Platelet Aggregation Inhibitors - pharmacology
Platelet Glycoprotein GPIb-IX Complex
Platelet Membrane Glycoproteins
Receptors, Immunologic - drug effects
Receptors, Immunologic - metabolism
Structure-Activity Relationship
title Potent inhibitors of platelet aggregation based upon the Arg-Gly-Asp-Phe sequence of fibrinogen. A proposal on the nature of the binding interaction between the Asp-carboxylate of RGDX mimetics and the platelet GP IIb-IIIa receptor
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